Job Description
7-month contract!
Required Skills & Experience
5+ years in a human factor engineering role 5+ years of experience in medical device development 5+ years hands on experience with labeling validation processes Familiarity with reprocessing workflows in MedTech (e.g., cleaning, disinfection, sterilization steps) Nice to Have Skills & Experience Experience in sterile reprocessing of medical devices, especially from a human factors perspective (not looking for ex-SPT turned HFE) Additional experience in labeling validation beyond core responsibilities Job Description An employer is seeking a Human Factors Engineer for an opportunity in the Cincinnati, OH area. This HFE will be responsible for collaborating with cross-functional teams (R&D, Regulatory, Quality) to ensure human factors are integrated throughout the product lifecycle, conducting usability evaluations and risk assessments related to labeling and reprocessing, supporting validation activities for labeling, including IFUs, packaging, and device markings. This HFE will be supporting a clinical trial and will be expected to analyze reprocessing workflows to identify usability risks and recommend design improvements as well as documenting findings and contribute to regulatory submissions (e.g., HF reports, validation protocols). Other day to day responsibilities will include participation in design reviews and provide HF input on product changes and new developments....management experience in Human Resources with prior experience in staffing and employee relations. Experience with Washington State Labor Law required. Previous manufacturing HR experience preferred. Experience handling highly confidential and sensitive...
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